SCN5A c.1713T>C ;(p.S571=)

Variant ID: 3-38645380-A-G

NM_000335.4(SCN5A):c.1713T>C;(p.S571=)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Diseases caused by mutations in Nav1.5 interacting proteins.

Cardiac Electrophysiology Clinics
Kyle, John W JW; Makielski, Jonathan C JC
Publication Date: 2014-12-01

Variant appearance in text: SCN5A: S571S
PubMed Link: 25395996
Variant Present in the following documents:
  • Main text
View BVdb publication page